Makson Healthcare quality laboratory

R&D & QUALITY

Quality Without Compromise.
Innovation Without Limits.

EU GMPEU GMP
TGA AustraliaTGA
Russia FDARussia FDA
WHO GMPWHO GMP
FSSAIFSSAI
US FDAUS FDA
HalalHalal
KosherKosher
Japan FDAJapan FDA
Ukraine FDAUkraine FDA
UAE FDAUAE FDA
Philippines FDAPhilippines FDA
EcoVadisEcovadis
SedexSedex
ULUL

From Concept to Shelf-Ready Product


Makson Healthcare's in-house R&D team works alongside production from day one. Our formulation scientists bring deep expertise across 7 dosage forms — developing products that meet global regulatory standards while optimising for taste, stability, and consumer appeal.

With dedicated pilot-scale equipment and European-grade BOSCH and Bühler production lines, we move from formulation to commercial manufacturing with no hand-offs, no gaps, and no delays.

The Development Journey

End-to-end support from concept through commercial manufacturing


01

Concept & Feasibility

Initial assessment of product concept, ingredient compatibility, and manufacturing feasibility.

02

Formulation Development

Prototype creation, excipient selection, taste optimisation, and active ingredient integration.

03

Stability Studies

ICH-condition stability testing including accelerated and long-term studies for tropical climates.

04

Pilot Batch Production

Small-scale production runs to validate formulation, process parameters, and product quality.

05

Scale-Up & Validation

Process validation at commercial scale with full documentation and quality sign-off.

06

Regulatory Support

Market-specific dossier preparation, registration support, and compliance documentation.

07

Commercial Manufacturing

Full-scale production with ongoing quality monitoring, batch consistency, and continuous improvement.

The Science Behind the Product


Taste Masking & Flavour Optimisation

Proprietary techniques to mask active ingredients while delivering consumer-preferred taste profiles across gummies, lozenges, and chocolates.

Stability for Tropical Climates

Deep expertise in Zone IV stability conditions, critical for products targeting APAC, Middle East, Africa, and Latin American markets.

Sugar-Free & Clean Label

Formulations using natural sweeteners, plant-based gelling agents, and clean-label ingredients to meet evolving consumer preferences.

Active Ingredient Integration

Precision dosing of vitamins, minerals, APIs, herbal extracts, and functional actives across all dosage forms.

Bioavailability Enhancement

Advanced delivery technologies to improve absorption and efficacy of active ingredients in consumer healthcare formats.

Custom Formats & Shapes

Custom moulds, dual-layer gummies, centre-fill formats, and unique shapes tailored to brand identity and consumer appeal.

QUALITY MANAGEMENT

Built Into Every Batch


Quality Assurance

  • Standard Operating Procedures (SOPs)
  • Change control and deviation management
  • CAPA (Corrective and Preventive Action)
  • Document management and batch record review
  • Supplier qualification and audit programmes

Quality Control

  • In-process and finished product testing
  • Stability studies (ICH conditions)
  • Microbiological testing and environmental monitoring
  • Analytical method development and validation
  • Raw material and packaging material testing

Regulatory Affairs

  • Market-specific dossier preparation
  • Registration and compliance support
  • EU, US, Australia, Middle East, and APAC expertise
  • Audit readiness and inspection support
  • Post-market surveillance documentation

European-Grade Machinery. Indian Manufacturing Scale.


BOSCH

European-engineered precision manufacturing lines for gummies, lozenges, and confectionery formats. Industry-leading accuracy, consistency, and throughput.

Bühler

Swiss-engineered chocolate processing technology for nutraceutical chocolate manufacturing. Decades of tempering and handling expertise at scale.

QC Laboratory

Fully equipped quality control laboratories with HPLC, dissolution testers, stability chambers, and microbiology suites across all facilities.

Certifications That Unlock Global Markets

Our comprehensive certification portfolio ensures your products can reach any market, anywhere in the world.


Europe

EU GMP certification enables direct market access across all European Union member states.

United States

US FDA registered facilities meeting cGMP requirements for the American market.

Australia & New Zealand

TGA (Therapeutic Goods Administration) approval for the Australian and New Zealand markets.

Middle East & Asia

Halal certification and WHO GMP compliance for Middle Eastern, Southeast Asian, and African markets.

Japan, Russia, Ukraine

Country-specific FDA registrations for regulated markets in Japan, Russia, and Ukraine.

Global Food Safety

FSSAI and Kosher certifications ensuring compliance with international food safety and dietary standards.

Ready to Start Your Formulation Project?

Let's discuss how Makson Healthcare can develop and manufacture your next product.

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